![Structural basis to repurpose boron-based proteasome inhibitors Bortezomib and Ixazomib as β-lactamase inhibitors | Scientific Reports Structural basis to repurpose boron-based proteasome inhibitors Bortezomib and Ixazomib as β-lactamase inhibitors | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-022-09392-6/MediaObjects/41598_2022_9392_Fig1_HTML.png)
Structural basis to repurpose boron-based proteasome inhibitors Bortezomib and Ixazomib as β-lactamase inhibitors | Scientific Reports
![Streamlined Process for the Chemical Synthesis of RNA Using 2′-O-Thionocarbamate-Protected Nucleoside Phosphoramidites in the Solid Phase | Journal of the American Chemical Society Streamlined Process for the Chemical Synthesis of RNA Using 2′-O-Thionocarbamate-Protected Nucleoside Phosphoramidites in the Solid Phase | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja201561z/asset/images/medium/ja-2011-01561z_0005.gif)
Streamlined Process for the Chemical Synthesis of RNA Using 2′-O-Thionocarbamate-Protected Nucleoside Phosphoramidites in the Solid Phase | Journal of the American Chemical Society
![Chemical structure of various blood antigens and antibody. a) O antigen... | Download Scientific Diagram Chemical structure of various blood antigens and antibody. a) O antigen... | Download Scientific Diagram](https://www.researchgate.net/publication/340217982/figure/fig1/AS:876613122138113@1586012263572/Chemical-structure-of-various-blood-antigens-and-antibody-a-O-antigen-b-A-antigen-c-B.jpg)
Chemical structure of various blood antigens and antibody. a) O antigen... | Download Scientific Diagram
![Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold | Nature Communications Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-023-38228-8/MediaObjects/41467_2023_38228_Fig1_HTML.png)
Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold | Nature Communications
![Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold | Nature Communications Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-023-38228-8/MediaObjects/41467_2023_38228_Fig4_HTML.png)
Direct nucleophilic and electrophilic activation of alcohols using a unified boron-based organocatalyst scaffold | Nature Communications
![Tetrahydroxydiboron‐Mediated Palladium‐Catalyzed Deoxygenative Transfer Hydrogenation of Aryl Ketones - Spaller - 2022 - Advanced Synthesis & Catalysis - Wiley Online Library Tetrahydroxydiboron‐Mediated Palladium‐Catalyzed Deoxygenative Transfer Hydrogenation of Aryl Ketones - Spaller - 2022 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/534c5f85-2415-4db9-8777-1c6032efbbb2/adsc202200482-toc-0001-m.jpg)
Tetrahydroxydiboron‐Mediated Palladium‐Catalyzed Deoxygenative Transfer Hydrogenation of Aryl Ketones - Spaller - 2022 - Advanced Synthesis & Catalysis - Wiley Online Library
![B–N, B–O, and B–CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes | Journal of the American Chemical Society B–N, B–O, and B–CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.6b05505/asset/images/large/ja-2016-05505e_0007.jpeg)
B–N, B–O, and B–CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes | Journal of the American Chemical Society
![Elucidating the Role of the Boronic Esters in the Suzuki–Miyaura Reaction: Structural, Kinetic, and Computational Investigations | Journal of the American Chemical Society Elucidating the Role of the Boronic Esters in the Suzuki–Miyaura Reaction: Structural, Kinetic, and Computational Investigations | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.8b00400/asset/images/medium/ja-2018-00400z_0028.gif)
Elucidating the Role of the Boronic Esters in the Suzuki–Miyaura Reaction: Structural, Kinetic, and Computational Investigations | Journal of the American Chemical Society
![Tri(1-adamantyl)phosphine: Expanding the Boundary of Electron-Releasing Character Available to Organophosphorus Compounds | Journal of the American Chemical Society Tri(1-adamantyl)phosphine: Expanding the Boundary of Electron-Releasing Character Available to Organophosphorus Compounds | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.6b03215/asset/images/large/ja-2016-03215m_0005.jpeg)
Tri(1-adamantyl)phosphine: Expanding the Boundary of Electron-Releasing Character Available to Organophosphorus Compounds | Journal of the American Chemical Society
![Hydrogen peroxide-activatable antioxidant prodrug as a targeted therapeutic agent for ischemia-reperfusion injury | Scientific Reports Hydrogen peroxide-activatable antioxidant prodrug as a targeted therapeutic agent for ischemia-reperfusion injury | Scientific Reports](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fsrep16592/MediaObjects/41598_2015_Article_BFsrep16592_Fig1_HTML.jpg)
Hydrogen peroxide-activatable antioxidant prodrug as a targeted therapeutic agent for ischemia-reperfusion injury | Scientific Reports
![Construction of boron-stereogenic compounds via enantioselective Cu-catalyzed desymmetric B–H bond insertion reaction | Nature Communications Construction of boron-stereogenic compounds via enantioselective Cu-catalyzed desymmetric B–H bond insertion reaction | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-022-30287-7/MediaObjects/41467_2022_30287_Fig1_HTML.png)
Construction of boron-stereogenic compounds via enantioselective Cu-catalyzed desymmetric B–H bond insertion reaction | Nature Communications
![Effects of Fe Electrolyte Impurities on Ni(OH)2/NiOOH Structure and Oxygen Evolution Activity | The Journal of Physical Chemistry C Effects of Fe Electrolyte Impurities on Ni(OH)2/NiOOH Structure and Oxygen Evolution Activity | The Journal of Physical Chemistry C](https://pubs.acs.org/cms/10.1021/acs.jpcc.5b00105/asset/images/medium/jp-2015-00105r_0009.gif)
Effects of Fe Electrolyte Impurities on Ni(OH)2/NiOOH Structure and Oxygen Evolution Activity | The Journal of Physical Chemistry C
![Reactive metal boride nanoparticles trap lipopolysaccharide and peptidoglycan for bacteria-infected wound healing | Nature Communications Reactive metal boride nanoparticles trap lipopolysaccharide and peptidoglycan for bacteria-infected wound healing | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-022-35050-6/MediaObjects/41467_2022_35050_Fig1_HTML.png)